NCT01126320
Completed
Not Applicable
Frequency of Ventilator Associated Pneumonia (VAP) in Mechanically Ventilated ICU Patients Using the AnapnoGuard System
Hospitech Respiration1 site in 1 country161 target enrollmentDecember 2010
ConditionsVentilator Associated Pneumonia
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Ventilator Associated Pneumonia
- Sponsor
- Hospitech Respiration
- Enrollment
- 161
- Locations
- 1
- Primary Endpoint
- VAP occurence
- Status
- Completed
- Last Updated
- 10 years ago
Overview
Brief Summary
Ventilator Associated Pneumonia (VAP) is a common complication experienced by mechanically ventilated patients and within the framework of Respiratory Intensive Care Units. The AnapnoGuard system, developed by Hospitech Respiration Ltd. is a ventilation guard system that includes a number of unique characteristics. This study was designed to test the frequency VAP in mechanically ventilated ICU patients using the AnapnoGuard System.
Investigators
Eligibility Criteria
Inclusion Criteria
- •ICU patients;
- •Patient was connected to AnapnoGuard system up to six hours from intubation;
- •Age - above 18.
Exclusion Criteria
- •Pneumonia;
- •Aspiration Pneumonia;
- •Chronic or Severe Pneumonia;
- •Chronic Obstructive Pulmonary Disease (COPD) requiring permanent home-based antibiotic treatment;
- •Interstitial Lung Disease (ILD);
- •Post Lung Transplant State;
- •Immunosuppression.
- •Patients ventilated in prone position
- •Patient who was ventilated 3 months prior to being enrolled in the study
- •Pregnant women
Outcomes
Primary Outcomes
VAP occurence
Time Frame: 2 years
Secondary Outcomes
- Adverse events occurence(2 years)
Study Sites (1)
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